medical MODERATE Updated 2026-05-20

GE Medical Systems, LLC recalls Revolution Ascend, computed tomography, Model Numbers 696900

See all recalls from GE Medical Systems, LLC →

Recalled Product

Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00840682146173; Serial Numbers: AS10G2200136YC AS10G2200101YC AS10G2200068YC AS10G2200035YC AS10G2300093YC AS10G2400094YC AS10G2400079YC AS10G2100008YC AS10G2500002YC CBDWG2400019HM CBDWG2300081HM AS10G2400056YC AS10G2400081YC AS10G2400087YC CBDWG2400117HM CBDWG2400085HM CBDWG2500003HM CBDWG2400140HM CBDWG2400126HM AS10G2200085YC AS10G2300057YC CBDWG2500011HM CBDWG2300056HM CBDWG2300041HM AS10G2300041YC

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Revolution Ascend, computed tomography, →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

INSPIREMD Inc recalls CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/

2026-06-17 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device (VAD) System Blood

2026-06-17 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

Abbott Medical recalls Merlin" Patient Care System (PCS) software Merlin" PCS 3650

2026-06-17 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

GE Medical Systems, LLC recalls Allia IGS 7 Pulse angiographic X-ray system

2026-06-17 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.